Pomfy M, Franko J
Department of Histology and Embryology, Faculty of Medicine, Safárik University, Kosice, Slovak Republic.
J Hirnforsch. 1999;39(4):465-71.
A new model of transient global cerebral ischemia in dogs with minimal measures of intervention is described together with a simple scale for evaluation of functional outcome. During pentobarbital anesthesia, a global cerebral ischemia lasting seven minutes was induced by a four-vessel occlusion and a controlled systemic hypotension. The reperfusion phase begun after removal of arterial clamps, and the animals were sacrificed by perfusion fixation 24 hours latter. The efficiency of controlled systemic hypotension in diminishing collateral blood flow was validated in two experimental groups with different cerebral filling pressure (CFP). Severe ischemia group (CFP 1.0-1.5 kPa) underwent near-complete ischemia as indicated by rCBF, electroencephalography, and histologically documented ischemic neuronal changes. Mild ischemia group (CFP 2.5-3 kPa) animals experienced reduction in cerebral blood flow well above the ischemic threshold, had better functional outcome as well as no ischemic neuronal changes on light microscopy. This model consistently produces global cerebral ischemia in dogs with minimal surgical intervention and pharmacological support, and without intracranial hypertension, cardiac arrest or asphyxia. We recommend this model for outcome-oriented studies of complete forebrain ischemia in dogs.
本文描述了一种在犬类中采用最少干预措施的短暂性全脑缺血新模型,并给出了一个用于评估功能转归的简单量表。在戊巴比妥麻醉期间,通过四血管闭塞和控制性全身低血压诱导持续7分钟的全脑缺血。在移除动脉夹后开始再灌注阶段,24小时后通过灌注固定法处死动物。在两个具有不同脑灌注压(CFP)的实验组中验证了控制性全身低血压在减少侧支血流方面的有效性。重度缺血组(CFP 1.0 - 1.5 kPa)如rCBF、脑电图及组织学记录的缺血性神经元变化所示,经历了近乎完全的缺血。轻度缺血组(CFP 2.5 - 3 kPa)的动物脑血流量减少程度远高于缺血阈值,功能转归更好,且在光学显微镜下无缺血性神经元变化。该模型通过最少的手术干预和药物支持,始终能在犬类中产生全脑缺血,且无颅内高压、心脏骤停或窒息情况。我们推荐此模型用于犬类全脑缺血的以结果为导向的研究。